Clinical Affairs

Company OverviewRegTrac is a leading healthcare regulatory partner specializing in Global Regulatory Affairs, Quality Systems, and Compliance for Medical Devices, Cosmetics, and Consumer Products. With expertise in navigating regulatory requirements across diverse markets, RegTrac empowers MedTech companies to innovate and expand globally while ensuring...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across...

Profile: Area Business Manager || Medical Device or Pharma SaleLocation: ChennaiExperience: 5-10 yearsSalary: Up to 13 LPAResponsibilities:Promote and sell Company's EMG Biofeedback Device and services within an assigned geographic area and/or specific customer accounts to meet or exceed sales targets.Develop, build, and strengthen long-term relationships...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Pharmacovigilance Project Lead to join our diverse and dynamic team. As a...

Pharmacovigilance Project LeadICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Pharmacovigilance Project Lead to join our...

Zonal Business Manager- Nephro DivisionDomnic Lewis has been mandated to hire for Zonal Business Manager- Nephro Division - ChennaiThe Zonal Business Manager (ZBM) is responsible for driving the successful execution of sales and marketing plans across their designated zone, with the objective of consistently achieving revenue targets. This leadership role...

Overview:The Regulatory Affairs Specialist position is responsible for RA/QA and co-ordinate with supply chain team, responsibilities includes but not least; maintaining of documentation, and support import requirements ensuring products released comply with import requirements.Support RA Manager for product registration and regulatory compliance and to...

EXECUTIVE**: **Experience**: TWO TO FOUR YEARS**: **Positions**: 1**: **Location**: Chennai**: **Qualification**: P.HD in Clinical Research**:

Dear Candidates, We have an opportunity with clinical trial development and CRO related assets and capabilities from an existing ACRO/SMO organization that is based in Chennai. We have over 10 years of experience running clinical trials as part of the global Group.  Position OverviewThe Head of Regulatory Affairs is responsible for providing strategic...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds. ClinChoice, is searching for an Executive - Regulatory Affairs (PLMDS) to join one of our clients. **Main Job Tasks and Responsibilities**: - Complete...

Job Summary The Regulatory Affairs Specialist is responsible for ensuring compliance with all applicable regulations governing the development, manufacturing, and distribution of the company's products. This role involves collaborating with internal teams and regulatory agencies to facilitate product registrations, approvals, and adherence to quality...

Location - Chennai, Pune, Mumbai, Delhi, Noida, Indore, Jaipur, Vijayawada, Meerut, Surat Designation - Clinical Specialist Business Unit - Infusion Therapy / Vascular Access Report to - Head Medical Affairs Dotted line reporting to - State Head Poly Medicure Limited (Polymed, Listed in NSE: BSE), is a leading medical device manufacturer and exporter from...

OverviewWe are seeking an experienced Associate Manager - CDM to support our clinical data management team in Chennai. The successful candidate will work as Subject Matter Expert (SME) for CRIO CTMS including e-Source creation, edit, oversee and mentor the end-to-end clinical trial management system activities, ensuring seamless integration between CTMS, EDC...

**Key Responsibilities**: - **Regulatory Compliance**: Ensure compliance with ISO 13485, EU MDR 2017/745, US-FDA, CDSCO, and other applicable international standards for medical devices. - **Submissions and Approvals**: Prepare, review, and submit regulatory documentation, including 510(k) and IMDR submissions, to regulatory authorities such as US-FDA,...

Summary 1 Conduct CME s seminars promotional events and In service programs in the respective region In order to improve BD SM value proposition amongst both clinical and economic buyers towards business outcome and achieve Regional business objectives 2 Clinical capability building amongst regional SM direct selling organisation and amongst channel partners...

Pepgra scientific editing and publication division serves clients across the globe. We offer editing, publication support, medical writing, translation, transcription, and researcher training services, to help individuals achieve their scientific communication goals. Pepgra employs a global team of highly skilled scientific editors, writers and peer...

Primary Skill - Managing the planning, coordination, and execution of User Acceptance Testing (UAT) for GxP applications across Pharma domains (Clinical Trial, Safety/Pharmacovigilance, Regulatory Affairs, Quality). The role ensures business requirements are validated, compliance is maintained (GxP, 21 CFR Part 11, GDPR, ICH, GAMP 5), and systems are fit for...